As medical devices become increasingly connected and software-driven, cybersecurity cannot be treated as a final compliance checkpoint. It must be integrated throughout the entire product lifecycle, from requirements and design to development, regulatory submission, and post-market support.

Join experts from PTC and MedCrypt to explore how MedTech manufacturers can embed cybersecurity into product development processes while improving collaboration across engineering, quality, regulatory, and security teams. Attendees will learn how end-to-end traceability and a lifecycle approach can help organizations address evolving FDA and European cybersecurity expectations, reduce risk, and deliver secure, compliant medical devices more efficiently.